46 results on '"Mein, C A"'
Search Results
2. Cytokine responses to exercise and activity in patients with chronic fatigue syndrome: case–control study
3. Evidence of a role for GTP cyclohydrolase-1 in visceral pain
4. Differences between disease-associated endoplasmic reticulum aminopeptidase 1 (ERAP1) isoforms in cellular expression, interactions with tumour necrosis factor receptor 1 (TNF-R1) and regulation by cytokines
5. 8.2 Cardiac Ion Channelopathies in Unexplained Stillbirths
6. Array-based DNA methylation profiling in follicular lymphoma
7. The EIF2AK3 gene region and type I diabetes in subjects from South India
8. Integrative mRNA profiling comparing cultured primary cells with clinical samples reveals PLK1 and C20orf20 as therapeutic targets in cutaneous squamous cell carcinoma
9. Array-based DNA methylation profiling in follicular lymphoma
10. Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi population
11. A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature
12. A new variation in the promoter region, the −604 C > T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance
13. Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis
14. Genetic Mechanisms of ABCA12 Mutation in Harlequin Ichthyosis
15. Filaggrin Mutation is not a Genetic Risk Factor for Atopic Dermatitis in the Bangladeshi Population
16. The South African "Bathing Suit Ichthyosis" is a Form of Lamellar Ichthyosis Caused by a Homozygous Missense Mutation, p.R315L, in Transglutaminase 1
17. Clinical and molecular features of harlequin ichthyosis: O-13
18. Methylome of human skeletal muscle after acute & chronic resistance exercise training, detraining & retraining
19. Systematic analysis of 123 candidate genes reveals two novel genes for hypertension
20. 936 Quantitative genome-wide methylation analysis of high-grade non-muscle invasive bladder cancer
21. P48 Prevalence And Determinants Of Vitamin D Deficiency In Asthma Patients
22. M145 Prevalence And Determinants Of Vitamin D Deficiency In Patients With Chronic Obstructive Pulmonary Disease
23. Association of the WNK1 gene with essential hypertension, blood pressure variability and serum and urine electrolytes
24. High quality genomic DNA extraction from postmortem fetal tissue
25. Genomic Deoxyribonucleic Acid Extraction from Post Mortem Fetal Tissue
26. Yes-associated protein (YAP) functions as a tumor suppressor in breast
27. A new variation in the promoter region, the −604 C>T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance
28. A Molecular Genetic and Statistical Approach for the Diagnosis of Dual-Site Cancers
29. NO ASSOCIATION OF THE WNK1 GENE WITH ESSENTIAL HYPERTENSION IN THE MRC BRIGHT STUDY
30. Genetics of essential hypertension
31. A new variation in the promoter region, the −604 C>T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance.
32. Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation.
33. Endogenous Aspergillus Endophthalmitis: Clinical Features and Treatment Outcomes
34. Relationship between external and internal calcium concentrations and prolactin cell activity in a euryhaline teleost
35. Loci on chromosomes 5p and 20q are linked to multiple hypertension phenotypes in the BRItish genetics of Hypertension (BRIGHT) study
36. Breast and ovarian carcinoma in the same patient, metastasis or dual primaries?
37. No association of the WNK1 gene with essential hypertension in the MRC BRIGHT study
38. Morphometrical study with light and electron -microscope o role in ionic regulation of 2 endocrine cell-types in stannius bodies of sticklebacks
39. `ome on the range
40. Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study
41. Multiple common variants for celiac disease influencing immune gene expression
42. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
43. A new variation in the promoter region, the -604 C>T, and the Leu72Met polymorphism of the ghrelin gene are associated with protection to insulin resistance.
44. Somatic mitochondrial DNA mutations in primary and metastatic ovarian cancer.
45. A search for type 1 diabetes susceptibility genes in families from the United Kingdom.
46. Quantification of X-chromosome inactivation patterns in haematological samples using the DNA PCR-based HUMARA assay.
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